Amyloid-related神经病变。

H H Goebel, J Bohl, S Störkel
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引用次数: 0

摘要

当骨髓瘤相关淀粉样蛋白(AL)沉积在免疫相关神经病变或家族性淀粉样蛋白多发性神经病变中,白蛋白前/转甲状腺素变异体以AF淀粉样蛋白沉积为标志时,可能会在周围神经内形成淀粉样蛋白,导致淀粉样蛋白相关神经病变。精细化的组织化学和最近的免疫组织化学技术确定了淀粉样蛋白的正确类型,从而确定了淀粉样蛋白相关神经病变的病理精确形式。神经病变是一种固有的思想,而不是强制性的临床和形态学成分在两种系统性淀粉样变性。成人形式的神经病变的多种致病因素,使得搜索淀粉样蛋白强制性每当各自的活检神经标本进行检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amyloid-related neuropathies.

Formation of amyloid within peripheral nerves, resulting in amyloid-related neuropathies, may occur when myeloma-associated amyloid (AL) is deposited in an immune-related neuropathy or in familial amyloid polyneuropathy where prealbumin/transthyretin variants are marked by AF amyloid deposition. Refined histochemical and recent immunohistochemical techniques identify the correct type of amyloid and thus the nosologically precise form of amyloid-related neuropathy. Neuropathy is an inherent thought not obligate clinical and morphological component in two of the three systemic amyloidoses. Multiple causative factors in adult forms of neuropathy render a search for amyloid mandatory whenever respective biopsied nerve specimens are examined.

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